@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP293283.RAsOm8vfIAn29Vf6V2t9jdZILBCMy4eqeoGMQ_234Uth8
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP293283.RAsOm8vfIAn29Vf6V2t9jdZILBCMy4eqeoGMQ_234Uth8130_head
{
this:
np:hasAssertion
dgn-np:NP293283.RAsOm8vfIAn29Vf6V2t9jdZILBCMy4eqeoGMQ_234Uth8130_assertion
;
np:hasProvenance
dgn-np:NP293283.RAsOm8vfIAn29Vf6V2t9jdZILBCMy4eqeoGMQ_234Uth8130_provenance
;
np:hasPublicationInfo
dgn-np:NP293283.RAsOm8vfIAn29Vf6V2t9jdZILBCMy4eqeoGMQ_234Uth8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP293283.RAsOm8vfIAn29Vf6V2t9jdZILBCMy4eqeoGMQ_234Uth8130_assertion
a
np:Assertion
.
dgn-np:NP293283.RAsOm8vfIAn29Vf6V2t9jdZILBCMy4eqeoGMQ_234Uth8130_provenance
a
np:Provenance
.
dgn-np:NP293283.RAsOm8vfIAn29Vf6V2t9jdZILBCMy4eqeoGMQ_234Uth8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP293283.RAsOm8vfIAn29Vf6V2t9jdZILBCMy4eqeoGMQ_234Uth8130_assertion
{
miriam-gene:6508
a
ncit:C16612
.
lld:C0026650
a
ncit:C7057
.
dgn-gda:DGNfd998d40931f4418ef44e7813e348dba
sio:SIO_000628
miriam-gene:6508
,
lld:C0026650
;
a
sio:SIO_001121
.
}
dgn-np:NP293283.RAsOm8vfIAn29Vf6V2t9jdZILBCMy4eqeoGMQ_234Uth8130_provenance
{
dgn-np:NP293283.RAsOm8vfIAn29Vf6V2t9jdZILBCMy4eqeoGMQ_234Uth8130_assertion
dcterms:description
"[In order to study the potential role of AE3 in human neurological disease, we characterized AE3 genomic structure and performed mutational analysis on patients with an episodic movement disorder that maps to the same genetic locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:10732805
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP293283.RAsOm8vfIAn29Vf6V2t9jdZILBCMy4eqeoGMQ_234Uth8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:47+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}